Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 373 |
| ensemblid | ENSG00000113595.15 |
| hgncid | 660 |
| symbol | TRIM23 |
| name | tripartite motif containing 23 |
| refseq_nuc | NM_001656.4 |
| refseq_prot | NP_001647.1 |
| ensembl_nuc | ENST00000231524.14 |
| ensembl_prot | ENSP00000231524.9 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 65589690 |
| end | 65624333 |
| strand | - |
| ver | v1.2 |
| region | chr5:65589690-65624333 |
| region5000 | chr5:65584690-65629333 |
| regionname0 | TRIM23_chr5_65589690_65624333 |
| regionname5000 | TRIM23_chr5_65584690_65629333 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 574 | 367 | 91 | 70 | 148 | 16 | 40 | 120 | TRIM23_chr5_65584690_65629333 | TRIM23 | MATLV others(569): Show |
chr5 | 65584690 | 65629333 |
| a0002 | 0/0 | 574 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | MATLV others(569): Show |
chr5 | 65584690 | 65629333 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1722 | 315 | 74 | 60 | 130 | 16 | 34 | TRIM23_chr5_65584690_65629333 | TRIM23 | ATGGC others(1717): Show |
chr5 | 65584690 | 65629333 | ||
| a0001c0002 | 0/1 | 1722 | 38 | 9 | 5 | 17 | 0 | 6 | TRIM23_chr5_65584690_65629333 | TRIM23 | ATGGC others(1717): Show |
chr5 | 65584690 | 65629333 | ||
| a0001c0003 | 0/0 | 1722 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | ATGGC others(1717): Show |
chr5 | 65584690 | 65629333 | ||
| a0001c0005 | 0/0 | 1722 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | ATGGC others(1717): Show |
chr5 | 65584690 | 65629333 | ||
| a0001c0006 | 0/0 | 1722 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | ATGGC others(1717): Show |
chr5 | 65584690 | 65629333 | ||
| a0001c0007 | 0/0 | 1722 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | ATGGC others(1717): Show |
chr5 | 65584690 | 65629333 | ||
| a0001c0008 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | ATGGC others(1717): Show |
chr5 | 65584690 | 65629333 | ||
| a0001c0009 | 0/0 | 1722 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | ATGGC others(1717): Show |
chr5 | 65584690 | 65629333 | ||
| a0002c0004 | 0/0 | 1722 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | ATGGC others(1717): Show |
chr5 | 65584690 | 65629333 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3863 | 122 | 17 | 25 | 60 | 7 | 12 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3858): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0002 | 0/0 | 3868 | 46 | 1 | 6 | 23 | 6 | 10 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3863): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0003 | 0/0 | 3866 | 36 | 13 | 7 | 10 | 3 | 3 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3861): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0004 | 0/0 | 3876 | 15 | 4 | 4 | 6 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3871): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0005 | 0/0 | 3868 | 12 | 8 | 0 | 4 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3863): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0007 | 0/0 | 3865 | 10 | 6 | 0 | 2 | 0 | 2 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3860): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0008 | 0/0 | 3878 | 10 | 3 | 2 | 3 | 0 | 2 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3873): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0009 | 0/0 | 3870 | 9 | 0 | 5 | 2 | 0 | 2 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3865): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0010 | 0/0 | 3870 | 7 | 7 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3865): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0012 | 0/0 | 3882 | 7 | 2 | 3 | 2 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3877): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0014 | 0/0 | 3880 | 4 | 1 | 1 | 2 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3875): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0016 | 0/0 | 3886 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3881): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0017 | 0/0 | 3862 | 3 | 0 | 1 | 2 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3857): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0018 | 0/0 | 3867 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3862): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0019 | 0/0 | 3874 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3869): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0020 | 0/0 | 3874 | 3 | 0 | 1 | 1 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3869): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0022 | 0/0 | 3864 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3859): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0023 | 0/0 | 3866 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3861): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0024 | 0/0 | 3866 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3861): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0028 | 0/0 | 3863 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3858): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0031 | 0/0 | 3866 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3861): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0032 | 0/0 | 3866 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3861): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0033 | 0/0 | 3868 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3863): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0034 | 0/0 | 3868 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3863): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0036 | 0/0 | 3872 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3867): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0037 | 0/0 | 3872 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3867): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0041 | 0/0 | 3878 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3873): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0043 | 0/0 | 3877 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3872): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0044 | 0/0 | 3878 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3873): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0045 | 0/0 | 3881 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3876): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0047 | 0/0 | 3884 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3879): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0048 | 0/0 | 3887 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3882): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0050 | 0/0 | 3892 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3887): Show |
chr5 | 65584690 | 65629333 |
| a0001c0001t0051 | 0/0 | 3894 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3889): Show |
chr5 | 65584690 | 65629333 |
| a0001c0002t0006 | 0/0 | 3877 | 12 | 3 | 2 | 2 | 0 | 5 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3872): Show |
chr5 | 65584690 | 65629333 |
| a0001c0002t0011 | 0/1 | 3879 | 7 | 1 | 1 | 3 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3874): Show |
chr5 | 65584690 | 65629333 |
| a0001c0002t0015 | 0/0 | 3881 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3876): Show |
chr5 | 65584690 | 65629333 |
| a0001c0002t0021 | 0/0 | 3883 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3878): Show |
chr5 | 65584690 | 65629333 |
| a0001c0002t0025 | 0/0 | 3875 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3870): Show |
chr5 | 65584690 | 65629333 |
| a0001c0002t0026 | 0/0 | 3877 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3872): Show |
chr5 | 65584690 | 65629333 |
| a0001c0002t0027 | 0/0 | 3885 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3880): Show |
chr5 | 65584690 | 65629333 |
| a0001c0002t0038 | 0/0 | 3873 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3868): Show |
chr5 | 65584690 | 65629333 |
| a0001c0002t0039 | 0/0 | 3873 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3868): Show |
chr5 | 65584690 | 65629333 |
| a0001c0002t0040 | 0/0 | 3875 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3870): Show |
chr5 | 65584690 | 65629333 |
| a0001c0002t0042 | 0/0 | 3877 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3872): Show |
chr5 | 65584690 | 65629333 |
| a0001c0002t0046 | 0/0 | 3880 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3875): Show |
chr5 | 65584690 | 65629333 |
| a0001c0002t0049 | 0/0 | 3889 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3884): Show |
chr5 | 65584690 | 65629333 |
| a0001c0003t0013 | 0/0 | 3869 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3864): Show |
chr5 | 65584690 | 65629333 |
| a0001c0003t0035 | 0/0 | 3871 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3866): Show |
chr5 | 65584690 | 65629333 |
| a0001c0005t0003 | 0/0 | 3866 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3861): Show |
chr5 | 65584690 | 65629333 |
| a0001c0005t0005 | 0/0 | 3868 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3863): Show |
chr5 | 65584690 | 65629333 |
| a0001c0006t0001 | 0/0 | 3863 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3858): Show |
chr5 | 65584690 | 65629333 |
| a0001c0007t0001 | 0/0 | 3863 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3858): Show |
chr5 | 65584690 | 65629333 |
| a0001c0008t0030 | 0/0 | 3863 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3858): Show |
chr5 | 65584690 | 65629333 |
| a0001c0009t0002 | 0/0 | 3868 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3863): Show |
chr5 | 65584690 | 65629333 |
| a0002c0004t0001 | 0/0 | 3863 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3858): Show |
chr5 | 65584690 | 65629333 |
| a0002c0004t0029 | 0/0 | 3862 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3857): Show |
chr5 | 65584690 | 65629333 |
| a0002c0004t0052 | 0/0 | 3862 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | AACCC others(3857): Show |
chr5 | 65584690 | 65629333 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 48 | 1 | 12 | 26 | 4 | 4 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0002g0002 | 0/0 | 14 | 0 | 0 | 6 | 2 | 6 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0002g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0002g0018 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0002g0052 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0002g0054 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0002g0056 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0002g0057 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0002g0059 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0003g0003 | 0/0 | 12 | 6 | 0 | 5 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0003g0016 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0003g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0004g0006 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0004g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0004g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0004g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0005g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0005g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0007g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0007g0012 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0007g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0008g0017 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0008g0046 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0008g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0008g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0009g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0009g0020 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0009g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0009g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0009g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0010g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0010g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0010g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0012g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0012g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0012g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0012g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0012g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0012g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0014g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0014g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0014g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0016g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0016g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0016g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0017g0055 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0017g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0018g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0018g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0019g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0019g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0019g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0020g0047 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0020g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0022g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0022g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0023g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0024g0058 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0028g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0031g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0032g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0033g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0034g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0036g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0037g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0041g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0043g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0044g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0045g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0047g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0048g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0050g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0001t0051g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0006g0008 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0006g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0006g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0006g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0006g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0006g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0011g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0011g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0011g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0011g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0011g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0011g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0011g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0015g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0015g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0015g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0015g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0021g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0021g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0025g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0025g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0026g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0027g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0038g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0039g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0040g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0042g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0046g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0002t0049g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0003t0013g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0003t0013g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0003t0013g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0003t0035g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0005t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0005t0005g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0006t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0006t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0007t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0008t0030g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0001c0009t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0002c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0002c0004t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0002c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0002c0004t0029g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| a0002c0004t0052g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | FIN | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0018 | EUR | FIN | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00408 | hp2 | a0001 | c0001 | t0014 | g0048 | EAS | CHS | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | CHS | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00609 | hp2 | a0001 | c0001 | t0047 | g0177 | EAS | CHS | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00642 | hp1 | a0001 | c0005 | t0003 | g0152 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00673 | hp2 | a0001 | c0001 | t0016 | g0204 | EAS | CHS | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG00741 | hp2 | a0001 | c0002 | t0006 | g0008 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01109 | hp1 | a0001 | c0002 | t0021 | g0042 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01167 | hp1 | a0001 | c0001 | t0037 | g0208 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0163 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01168 | hp1 | a0001 | c0005 | t0005 | g0036 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01168 | hp2 | a0001 | c0001 | t0008 | g0046 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01169 | hp1 | a0001 | c0001 | t0020 | g0209 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0017 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01175 | hp1 | a0001 | c0005 | t0005 | g0036 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01243 | hp2 | a0001 | c0006 | t0001 | g0075 | AMR | PUR | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01255 | hp1 | a0001 | c0001 | t0032 | g0210 | AMR | CLM | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01256 | hp1 | a0001 | c0001 | t0012 | g0049 | AMR | CLM | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01256 | hp2 | a0001 | c0002 | t0042 | g0125 | AMR | CLM | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01258 | hp2 | a0001 | c0001 | t0012 | g0171 | AMR | CLM | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0153 | AMR | CLM | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01261 | hp2 | a0001 | c0001 | t0022 | g0149 | AMR | CLM | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0174 | AMR | CLM | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01361 | hp2 | a0001 | c0009 | t0002 | g0207 | AMR | CLM | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01433 | hp2 | a0001 | c0001 | t0024 | g0058 | AMR | CLM | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01496 | hp2 | a0001 | c0001 | t0009 | g0200 | AMR | CLM | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0205 | EUR | IBS | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | IBS | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0016 | EUR | IBS | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0016 | EUR | IBS | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0054 | EUR | IBS | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01884 | hp1 | a0001 | c0008 | t0030 | g0073 | AFR | ACB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0214 | AFR | ACB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01928 | hp1 | a0001 | c0001 | t0009 | g0019 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01943 | hp2 | a0001 | c0001 | t0009 | g0198 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01952 | hp1 | a0001 | c0002 | t0011 | g0126 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01975 | hp1 | a0001 | c0001 | t0009 | g0019 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01993 | hp1 | a0001 | c0001 | t0014 | g0048 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01993 | hp2 | a0001 | c0001 | t0009 | g0019 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02004 | hp2 | a0001 | c0001 | t0012 | g0049 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02027 | hp1 | a0001 | c0001 | t0008 | g0182 | EAS | KHV | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02040 | hp1 | a0001 | c0001 | t0034 | g0203 | EAS | KHV | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02040 | hp2 | a0001 | c0001 | t0016 | g0050 | EAS | KHV | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0183 | AFR | ACB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0156 | AFR | ACB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02083 | hp2 | a0001 | c0002 | t0040 | g0131 | EAS | KHV | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02129 | hp1 | a0001 | c0002 | t0006 | g0132 | EAS | KHV | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | KHV | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0213 | AFR | ACB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02145 | hp2 | a0001 | c0002 | t0011 | g0136 | AFR | ACB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02148 | hp1 | a0001 | c0002 | t0006 | g0133 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CDX | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0078 | AFR | ACB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0145 | AFR | ACB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02258 | hp2 | a0001 | c0001 | t0018 | g0041 | AFR | ACB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0192 | AFR | ACB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02280 | hp2 | a0001 | c0003 | t0013 | g0011 | AFR | ACB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02293 | hp1 | a0001 | c0001 | t0024 | g0058 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | ACB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02572 | hp1 | a0001 | c0003 | t0013 | g0070 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0217 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02602 | hp1 | a0001 | c0001 | t0009 | g0020 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02602 | hp2 | a0001 | c0001 | t0007 | g0012 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02622 | hp1 | a0001 | c0001 | t0019 | g0215 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02630 | hp1 | a0001 | c0002 | t0006 | g0008 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02630 | hp2 | a0002 | c0004 | t0001 | g0060 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0216 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02647 | hp2 | a0001 | c0001 | t0010 | g0005 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02698 | hp1 | a0001 | c0002 | t0006 | g0033 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02723 | hp1 | a0001 | c0002 | t0006 | g0008 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02723 | hp2 | a0001 | c0001 | t0012 | g0186 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02735 | hp1 | a0001 | c0002 | t0006 | g0121 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02738 | hp2 | a0001 | c0002 | t0006 | g0135 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02809 | hp1 | a0001 | c0003 | t0013 | g0011 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02809 | hp2 | a0001 | c0001 | t0036 | g0146 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02818 | hp2 | a0001 | c0001 | t0031 | g0162 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0164 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02895 | hp1 | a0001 | c0001 | t0010 | g0005 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02895 | hp2 | a0001 | c0001 | t0012 | g0191 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02896 | hp1 | a0001 | c0002 | t0027 | g0043 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02897 | hp1 | a0001 | c0002 | t0027 | g0043 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02897 | hp2 | a0001 | c0001 | t0010 | g0005 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02922 | hp1 | a0001 | c0001 | t0019 | g0143 | AFR | ESN | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0039 | AFR | ESN | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02965 | hp2 | a0002 | c0004 | t0001 | g0065 | AFR | ESN | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | ESN | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | ESN | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02976 | hp2 | a0001 | c0003 | t0013 | g0071 | AFR | ESN | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03041 | hp1 | a0001 | c0001 | t0018 | g0167 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03098 | hp1 | a0002 | c0004 | t0052 | g0066 | AFR | MSL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | ESN | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03130 | hp2 | a0002 | c0004 | t0001 | g0068 | AFR | ESN | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0005 | AFR | ESN | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | ESN | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03195 | hp1 | a0001 | c0001 | t0051 | g0184 | AFR | ESN | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03195 | hp2 | a0001 | c0001 | t0019 | g0147 | AFR | ESN | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0039 | AFR | MSL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03209 | hp2 | a0001 | c0001 | t0014 | g0189 | AFR | MSL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03225 | hp1 | a0001 | c0006 | t0001 | g0074 | AFR | MSL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03225 | hp2 | a0001 | c0002 | t0021 | g0170 | AFR | MSL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03239 | hp1 | a0001 | c0001 | t0009 | g0020 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03239 | hp2 | a0001 | c0002 | t0011 | g0137 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03453 | hp2 | a0002 | c0004 | t0029 | g0064 | AFR | MSL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0077 | AFR | MSL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0144 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03516 | hp1 | a0001 | c0001 | t0010 | g0005 | AFR | ESN | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0193 | AFR | ESN | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | GWD | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03579 | hp2 | a0001 | c0003 | t0035 | g0072 | AFR | MSL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03669 | hp2 | a0001 | c0001 | t0020 | g0047 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03688 | hp2 | a0001 | c0002 | t0006 | g0033 | SAS | STU | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03710 | hp1 | a0001 | c0001 | t0033 | g0195 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | BEB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | BEB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | BEB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG04184 | hp1 | a0001 | c0001 | t0008 | g0172 | SAS | BEB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG04204 | hp1 | a0001 | c0001 | t0008 | g0017 | SAS | STU | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG04228 | hp1 | a0001 | c0002 | t0006 | g0129 | SAS | STU | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG04228 | hp2 | a0001 | c0001 | t0007 | g0012 | SAS | STU | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0069 | AFR | YRI | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18522 | hp2 | a0001 | c0001 | t0050 | g0188 | AFR | YRI | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18906 | hp1 | a0001 | c0002 | t0049 | g0169 | AFR | YRI | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18906 | hp2 | a0001 | c0001 | t0010 | g0139 | AFR | YRI | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18942 | hp2 | a0001 | c0001 | t0008 | g0017 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18947 | hp1 | a0001 | c0001 | t0014 | g0178 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18947 | hp2 | a0001 | c0001 | t0044 | g0212 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18949 | hp1 | a0001 | c0001 | t0008 | g0046 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18953 | hp1 | a0001 | c0007 | t0001 | g0086 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18953 | hp2 | a0001 | c0001 | t0020 | g0047 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18954 | hp1 | a0001 | c0002 | t0011 | g0117 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18957 | hp2 | a0001 | c0002 | t0038 | g0122 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18959 | hp1 | a0001 | c0002 | t0011 | g0119 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18962 | hp1 | a0001 | c0001 | t0009 | g0202 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18963 | hp2 | a0001 | c0002 | t0015 | g0118 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18964 | hp1 | a0001 | c0002 | t0015 | g0127 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18966 | hp2 | a0001 | c0002 | t0015 | g0138 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18969 | hp2 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18973 | hp1 | a0001 | c0001 | t0022 | g0168 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18973 | hp2 | a0001 | c0002 | t0025 | g0124 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18974 | hp2 | a0001 | c0001 | t0043 | g0176 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18979 | hp2 | a0001 | c0002 | t0046 | g0128 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18991 | hp1 | a0001 | c0001 | t0023 | g0040 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19000 | hp1 | a0001 | c0001 | t0005 | g0159 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19001 | hp1 | a0001 | c0002 | t0011 | g0130 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19002 | hp1 | a0001 | c0002 | t0026 | g0032 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19007 | hp1 | a0001 | c0001 | t0007 | g0100 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19007 | hp2 | a0001 | c0001 | t0007 | g0012 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19012 | hp2 | a0001 | c0001 | t0023 | g0040 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | LWK | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0185 | AFR | LWK | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19054 | hp1 | a0001 | c0001 | t0017 | g0055 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19057 | hp2 | a0001 | c0001 | t0012 | g0180 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19058 | hp2 | a0001 | c0001 | t0012 | g0175 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19067 | hp2 | a0001 | c0002 | t0026 | g0032 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19074 | hp2 | a0001 | c0001 | t0005 | g0155 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19075 | hp1 | a0001 | c0002 | t0015 | g0116 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19078 | hp1 | a0001 | c0001 | t0009 | g0020 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19081 | hp1 | a0001 | c0001 | t0017 | g0197 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19081 | hp2 | a0001 | c0001 | t0016 | g0173 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19082 | hp1 | a0001 | c0002 | t0006 | g0134 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19084 | hp1 | a0001 | c0001 | t0028 | g0094 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19086 | hp1 | a0001 | c0001 | t0016 | g0050 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19087 | hp2 | a0001 | c0001 | t0045 | g0181 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19089 | hp2 | a0001 | c0002 | t0025 | g0120 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19240 | hp1 | a0001 | c0001 | t0018 | g0041 | AFR | YRI | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ASW | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ASW | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0142 | EUR | TSI | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0211 | EUR | TSI | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | GIH | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01123 | hp1 | a0001 | c0001 | t0017 | g0055 | AMR | CLM | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0190 | AFR | ACB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02109 | hp2 | a0001 | c0003 | t0013 | g0011 | AFR | ACB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0148 | AFR | ACB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02486 | hp2 | a0001 | c0002 | t0006 | g0008 | AFR | ACB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02559 | hp1 | a0001 | c0001 | t0041 | g0140 | AFR | ACB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0154 | AFR | ACB | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | USA | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| HG06807 | hp2 | a0001 | c0002 | t0021 | g0042 | AFR | USA | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18955 | hp1 | a0001 | c0002 | t0039 | g0123 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | USA | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | USA | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | LWK | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| NA21309 | hp2 | a0001 | c0001 | t0048 | g0187 | AFR | LWK | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0011 | g0115 | REF | REF | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | TRIM23_chr5_65584690_65629333 | TRIM23 | chr5 | 65584690 | 65629333 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:65591860 | C | G | 1 | a0002 | 5 | HG02630.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
missense_variant | MODERATE | c.1634G>C | p.Gly545Ala | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 1693/3863 | 1634/1725 | 545/574 | chr5 | 65591860 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:65591787 | T | C | 1 | a0001c0005 | 3 | HG00642.hp1 HG01168.hp1 HG01175.hp1 |
synonymous_variant | LOW | c.1707A>G | p.Gly569Gly | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 1766/3863 | 1707/1725 | 569/574 | chr5 | 65591787 | |||
| chr5:65597112 | T | G | 1 | a0001c0002 | 37 | HG00741.hp2 HG01109.hp1 HG01256.hp2 others(34): Show |
synonymous_variant | LOW | c.1248A>C | p.Gly416Gly | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 8/11 | 1307/3863 | 1248/1725 | 416/574 | chr5 | 65597112 | |||
| chr5:65609366 | T | A | 1 | a0001c0008 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.921A>T | p.Leu307Leu | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/11 | 980/3863 | 921/1725 | 307/574 | chr5 | 65609366 | |||
| chr5:65609429 | T | C | 1 | a0001c0009 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.858A>G | p.Ser286Ser | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/11 | 917/3863 | 858/1725 | 286/574 | chr5 | 65609429 | |||
| chr5:65609447 | A | G | 1 | a0001c0003 | 6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
synonymous_variant | LOW | c.840T>C | p.Thr280Thr | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/11 | 899/3863 | 840/1725 | 280/574 | chr5 | 65609447 | |||
| chr5:65611755 | G | T | 1 | a0001c0007 | 1 | NA18953.hp1 | synonymous_variant | LOW | c.493C>A | p.Arg165Arg | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 4/11 | 552/3863 | 493/1725 | 165/574 | chr5 | 65611755 | |||
| chr5:65611828 | A | T | 1 | a0001c0006 | 2 | HG01243.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.420T>A | p.Thr140Thr | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 4/11 | 479/3863 | 420/1725 | 140/574 | chr5 | 65611828 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:65589785 | G | A | 1 | a0001c0001t0023 | 2 | NA18991.hp1 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1984C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 1984 | chr5 | 65589785 | ||||||
| chr5:65589840 | T | C | 1 | a0001c0001t0031 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1929A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 1929 | chr5 | 65589840 | ||||||
| chr5:65590047 | C | A | 1 | a0001c0001t0034 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1722G>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 1722 | chr5 | 65590047 | ||||||
| chr5:65590057 | A | G | 1 | a0001c0002t0027 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1712T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 1712 | chr5 | 65590057 | ||||||
| chr5:65590058 | C | T | 47 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(44): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*1711G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 1711 | chr5 | 65590058 | ||||||
| chr5:65590152 | C | A | 1 | a0001c0001t0041 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1617G>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 1617 | chr5 | 65590152 | ||||||
| chr5:65590212 | C | T | 1 | a0001c0001t0032 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1557G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 1557 | chr5 | 65590212 | ||||||
| chr5:65590218 | T | C | 3 | a0001c0002t0026 a0001c0002t0039 a0001c0002t0040 |
4 | HG02083.hp2 NA18955.hp1 NA19002.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1551A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 1551 | chr5 | 65590218 | ||||||
| chr5:65590250 | C | T | 1 | a0001c0008t0030 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1519G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 1519 | chr5 | 65590250 | ||||||
| chr5:65590486 | C | T | 1 | a0001c0008t0030 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1283G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 1283 | chr5 | 65590486 | ||||||
| chr5:65590547 | TA | T | 48 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(45): Show |
222 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*1221delT | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 1221 | chr5 | 65590547 | ||||||
| chr5:65590587 | G | A | 1 | a0001c0002t0046 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1182C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 1182 | chr5 | 65590587 | ||||||
| chr5:65590621 | A | C | 1 | a0001c0001t0041 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1148T>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 1148 | chr5 | 65590621 | ||||||
| chr5:65590683 | AT | A | 13 | a0001c0002t0006 a0001c0002t0011 a0001c0002t0015 others(10): Show |
37 | HG00741.hp2 HG01109.hp1 HG01256.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1085delA | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 1085 | chr5 | 65590683 | ||||||
| chr5:65590719 | A | G | 11 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0010 others(8): Show |
70 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1050T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 1050 | chr5 | 65590719 | ||||||
| chr5:65591230 | T | A | 1 | a0001c0002t0042 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*539A>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 539 | chr5 | 65591230 | ||||||
| chr5:65591356 | A | C | 1 | a0001c0001t0033 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*413T>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 413 | chr5 | 65591356 | ||||||
| chr5:65591385 | G | C | 1 | a0001c0002t0040 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*384C>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 384 | chr5 | 65591385 | ||||||
| chr5:65591410 | C | T | 1 | a0001c0001t0028 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*359G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 359 | chr5 | 65591410 | ||||||
| chr5:65591643 | C | CTATATAT others(9): Show |
1 | a0001c0001t0044 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*125_*126insTATATA others(10): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 125 | chr5 | 65591643 | ||||||
| chr5:65591645 | T | A | 1 | a0001c0001t0044 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*124A>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 124 | chr5 | 65591645 | ||||||
| chr5:65591645 | T | TATATATA others(8): Show |
1 | a0001c0001t0043 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*123_*124insTATATA others(9): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 123 | chr5 | 65591645 | ||||||
| chr5:65591645 | T | TATATATA others(12): Show |
2 | a0001c0001t0045 a0001c0002t0046 |
2 | NA18979.hp2 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*123_*124insTATATA others(13): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 123 | chr5 | 65591645 | ||||||
| chr5:65591645 | T | TATATATA others(18): Show |
1 | a0001c0001t0048 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*123_*124insTATATA others(19): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 123 | chr5 | 65591645 | ||||||
| chr5:65591645 | T | TTA | 2 | a0001c0001t0007 a0001c0001t0022 |
12 | HG01261.hp2 HG02257.hp2 HG02602.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*122_*123dupTA | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 123 | chr5 | 65591645 | ||||||
| chr5:65591645 | T | TTATA | 7 | a0001c0001t0003 a0001c0001t0018 a0001c0001t0023 others(4): Show |
46 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*120_*123dupTATA | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 123 | chr5 | 65591645 | ||||||
| chr5:65591645 | T | TTATATA | 7 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0033 others(4): Show |
68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*118_*123dupTATATA | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 123 | chr5 | 65591645 | ||||||
| chr5:65591645 | T | TTATATAT others(1): Show |
3 | a0001c0001t0009 a0001c0001t0010 a0001c0003t0035 |
17 | HG01496.hp2 HG01928.hp1 HG01943.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*116_*123dupTATATA others(2): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 123 | chr5 | 65591645 | ||||||
| chr5:65591645 | T | TTATATAT others(3): Show |
2 | a0001c0001t0036 a0001c0001t0037 |
2 | HG01167.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*114_*123dupTATATA others(4): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 123 | chr5 | 65591645 | ||||||
| chr5:65591645 | T | TTATATAT others(5): Show |
4 | a0001c0001t0019 a0001c0001t0020 a0001c0002t0038 others(1): Show |
8 | HG01169.hp1 HG02622.hp1 HG02922.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*112_*123dupTATATA others(6): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 123 | chr5 | 65591645 | ||||||
| chr5:65591645 | T | TTATATAT others(7): Show |
3 | a0001c0001t0004 a0001c0002t0025 a0001c0002t0040 |
18 | HG01069.hp1 HG01071.hp1 HG01358.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*110_*123dupTATATA others(8): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 123 | chr5 | 65591645 | ||||||
| chr5:65591645 | T | TTATATAT others(9): Show |
5 | a0001c0001t0008 a0001c0001t0041 a0001c0002t0006 others(2): Show |
26 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*108_*123dupTATATA others(10): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 123 | chr5 | 65591645 | ||||||
| chr5:65591645 | T | TTATATAT others(11): Show |
2 | a0001c0001t0014 a0001c0002t0011 |
10 | HG00408.hp2 HG01952.hp1 HG01993.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*106_*123dupTATATA others(12): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 123 | chr5 | 65591645 | ||||||
| chr5:65591645 | T | TTATATAT others(13): Show |
2 | a0001c0001t0012 a0001c0002t0015 |
11 | HG01256.hp1 HG01258.hp2 HG02004.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*104_*123dupTATATA others(14): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 123 | chr5 | 65591645 | ||||||
| chr5:65591645 | T | TTATATAT others(15): Show |
2 | a0001c0001t0047 a0001c0002t0021 |
4 | HG00609.hp2 HG01109.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*123_*124insTATATA others(16): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 123 | chr5 | 65591645 | ||||||
| chr5:65591645 | T | TTATATAT others(17): Show |
2 | a0001c0001t0016 a0001c0002t0027 |
6 | HG00673.hp2 HG02040.hp2 HG02896.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*123_*124insTATATA others(18): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 123 | chr5 | 65591645 | ||||||
| chr5:65591645 | T | TTATATAT others(21): Show |
1 | a0001c0002t0049 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*123_*124insTATATA others(22): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 123 | chr5 | 65591645 | ||||||
| chr5:65591645 | T | TTATATAT others(23): Show |
1 | a0001c0001t0050 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*123_*124insTATATA others(24): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 123 | chr5 | 65591645 | ||||||
| chr5:65591645 | T | TTATATAT others(25): Show |
1 | a0001c0001t0051 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*123_*124insTATATA others(26): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 123 | chr5 | 65591645 | ||||||
| chr5:65591656 | T | C | 1 | a0002c0004t0052 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*113A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 11/11 | 113 | chr5 | 65591656 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:65592001 | C | G | 5 | a0001c0001t0010g0005 a0001c0001t0010g0148 a0001c0001t0019g0143 others(2): Show |
9 | HG02486.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1546-53G>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65592001 | |||||||
| chr5:65592072 | C | G | 4 | a0001c0003t0013g0011 a0001c0003t0013g0070 a0001c0003t0013g0071 others(1): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1546-124G>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65592072 | |||||||
| chr5:65592088 | T | G | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1546-140A>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65592088 | |||||||
| chr5:65592228 | A | G | 1 | a0001c0001t0041g0140 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1546-280T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65592228 | |||||||
| chr5:65592244 | G | A | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1546-296C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65592244 | |||||||
| chr5:65592258 | C | G | 1 | a0001c0001t0007g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1546-310G>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65592258 | |||||||
| chr5:65592312 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1546-364C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65592312 | |||||||
| chr5:65592372 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1546-424C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65592372 | |||||||
| chr5:65592519 | G | A | 1 | a0001c0008t0030g0073 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1546-571C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65592519 | |||||||
| chr5:65592550 | T | TA | 4 | a0001c0003t0013g0011 a0001c0003t0013g0070 a0001c0003t0013g0071 others(1): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1546-603dupT | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65592550 | |||||||
| chr5:65592578 | C | T | 2 | a0001c0006t0001g0074 a0001c0006t0001g0075 |
2 | HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1546-630G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65592578 | |||||||
| chr5:65592702 | C | A | 1 | a0001c0001t0003g0153 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1546-754G>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65592702 | |||||||
| chr5:65592823 | C | T | 1 | a0002c0004t0001g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1546-875G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65592823 | |||||||
| chr5:65592968 | A | G | 4 | a0001c0002t0021g0042 a0001c0002t0021g0170 a0001c0002t0027g0043 others(1): Show |
6 | HG01109.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1546-1020T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65592968 | |||||||
| chr5:65593044 | C | CT | 33 | a0001c0001t0004g0006 a0001c0001t0004g0044 a0001c0001t0004g0045 others(30): Show |
47 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.1546-1097dupA | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65593044 | |||||||
| chr5:65593160 | C | T | 2 | a0001c0001t0007g0010 a0001c0001t0007g0069 |
4 | HG02970.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1546-1212G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65593160 | |||||||
| chr5:65593164 | G | C | 1 | a0001c0001t0007g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1546-1216C>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65593164 | |||||||
| chr5:65593214 | C | G | 30 | a0001c0002t0006g0008 a0001c0002t0006g0033 a0001c0002t0006g0121 others(27): Show |
37 | HG00741.hp2 HG01109.hp1 HG01256.hp2 others(34): Show |
intron_variant | MODIFIER | c.1546-1266G>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65593214 | |||||||
| chr5:65593252 | C | T | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1545+1269G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65593252 | |||||||
| chr5:65593264 | G | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0206 a0001c0001t0009g0202 |
9 | HG00423.hp1 NA18962.hp1 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.1545+1257C>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65593264 | |||||||
| chr5:65593298 | G | C | 1 | a0001c0002t0006g0129 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1545+1223C>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65593298 | |||||||
| chr5:65593350 | G | A | 1 | a0001c0001t0001g0023 | 2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1545+1171C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65593350 | |||||||
| chr5:65593446 | G | A | 2 | a0001c0001t0007g0010 a0001c0001t0007g0069 |
4 | HG02970.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1545+1075C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65593446 | |||||||
| chr5:65593808 | G | A | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1545+713C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65593808 | |||||||
| chr5:65594002 | G | A | 1 | a0001c0001t0003g0154 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1545+519C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65594002 | |||||||
| chr5:65594006 | G | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0067 |
4 | HG02451.hp2 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1545+515C>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65594006 | |||||||
| chr5:65594123 | C | T | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1545+398G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65594123 | |||||||
| chr5:65594190 | A | C | 26 | a0001c0002t0006g0008 a0001c0002t0006g0033 a0001c0002t0006g0121 others(23): Show |
31 | HG00741.hp2 HG01256.hp2 HG01952.hp1 others(28): Show |
intron_variant | MODIFIER | c.1545+331T>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65594190 | |||||||
| chr5:65594302 | A | C | 3 | a0001c0001t0009g0019 a0001c0001t0009g0198 a0001c0001t0009g0200 |
5 | HG01496.hp2 HG01928.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1545+219T>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65594302 | |||||||
| chr5:65594388 | A | G | 4 | a0001c0003t0013g0011 a0001c0003t0013g0070 a0001c0003t0013g0071 others(1): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1545+133T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65594388 | |||||||
| chr5:65594466 | C | T | 2 | a0001c0001t0003g0141 a0001c0001t0003g0151 |
2 | NA18948.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1545+55G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 10/10 | chr5 | 65594466 | |||||||
| chr5:65594652 | A | C | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
splice_region_variant&intron_variant | LOW | c.1421-7T>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65594652 | |||||||
| chr5:65594661 | T | A | 1 | a0001c0001t0008g0182 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1421-16A>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65594661 | |||||||
| chr5:65594783 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1421-138C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65594783 | |||||||
| chr5:65594792 | G | A | 1 | a0001c0001t0007g0069 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1421-147C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65594792 | |||||||
| chr5:65594881 | A | G | 5 | a0002c0004t0001g0060 a0002c0004t0001g0065 a0002c0004t0001g0068 others(2): Show |
5 | HG02630.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1421-236T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65594881 | |||||||
| chr5:65594991 | T | C | 4 | a0001c0003t0013g0011 a0001c0003t0013g0070 a0001c0003t0013g0071 others(1): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1421-346A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65594991 | |||||||
| chr5:65595108 | C | T | 1 | a0001c0001t0007g0078 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1421-463G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65595108 | |||||||
| chr5:65595119 | A | C | 1 | a0001c0001t0012g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1421-474T>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65595119 | |||||||
| chr5:65595210 | G | A | 1 | a0001c0001t0003g0154 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1421-565C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65595210 | |||||||
| chr5:65595227 | T | C | 1 | a0001c0001t0001g0028 | 2 | NA18949.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1421-582A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65595227 | |||||||
| chr5:65595245 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1421-600T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65595245 | |||||||
| chr5:65595420 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1421-775A>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65595420 | |||||||
| chr5:65595423 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1421-778A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65595423 | |||||||
| chr5:65595425 | G | T | 1 | a0001c0001t0001g0092 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1421-780C>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65595425 | |||||||
| chr5:65595490 | G | A | 4 | a0001c0003t0013g0011 a0001c0003t0013g0070 a0001c0003t0013g0071 others(1): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1421-845C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65595490 | |||||||
| chr5:65595552 | G | T | 3 | a0001c0002t0021g0042 a0001c0002t0021g0170 a0001c0002t0049g0169 |
4 | HG01109.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1420+869C>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65595552 | |||||||
| chr5:65595557 | C | CA | 6 | a0001c0001t0001g0031 a0001c0001t0001g0080 a0001c0001t0001g0096 others(3): Show |
9 | HG02148.hp2 HG02970.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.1420+863dupT | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65595557 | |||||||
| chr5:65595557 | CA | C | 134 | a0001c0001t0001g0091 a0001c0001t0001g0109 a0001c0001t0002g0002 others(131): Show |
214 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1420+863delT | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65595557 | |||||||
| chr5:65595557 | CAA | C | 6 | a0001c0001t0002g0201 a0001c0001t0009g0200 a0001c0001t0018g0167 others(3): Show |
6 | HG01496.hp2 HG02735.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1420+862_1420+863d others(4): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65595557 | |||||||
| chr5:65595582 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1420+839C>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65595582 | |||||||
| chr5:65595612 | A | G | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1420+809T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65595612 | |||||||
| chr5:65595725 | C | CA | 141 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(138): Show |
222 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.1420+695dupT | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65595725 | |||||||
| chr5:65596118 | T | C | 2 | a0001c0001t0007g0010 a0001c0001t0007g0069 |
4 | HG02970.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1420+303A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65596118 | |||||||
| chr5:65596147 | C | T | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1420+274G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65596147 | |||||||
| chr5:65596200 | G | A | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1420+221C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65596200 | |||||||
| chr5:65596225 | G | A | 1 | a0001c0002t0011g0119 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1420+196C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65596225 | |||||||
| chr5:65596292 | AC | A | 2 | a0001c0001t0005g0039 a0001c0001t0005g0145 |
3 | HG02258.hp1 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1420+128delG | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65596292 | |||||||
| chr5:65596323 | C | T | 1 | a0001c0001t0003g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1420+98G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65596323 | |||||||
| chr5:65596364 | C | A | 1 | a0001c0001t0014g0178 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1420+57G>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65596364 | |||||||
| chr5:65596377 | C | T | 2 | a0001c0001t0005g0035 a0001c0001t0005g0155 |
3 | NA18946.hp1 NA18969.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1420+44G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 9/10 | chr5 | 65596377 | |||||||
| chr5:65596605 | C | A | 14 | a0001c0001t0005g0039 a0001c0001t0005g0145 a0001c0001t0005g0156 others(11): Show |
19 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1310-74G>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 8/10 | chr5 | 65596605 | |||||||
| chr5:65596688 | G | A | 155 | a0001c0001t0001g0023 a0001c0001t0001g0076 a0001c0001t0002g0002 others(152): Show |
241 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1310-157C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 8/10 | chr5 | 65596688 | |||||||
| chr5:65596784 | A | T | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1310-253T>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 8/10 | chr5 | 65596784 | |||||||
| chr5:65596859 | T | C | 2 | a0001c0006t0001g0074 a0001c0006t0001g0075 |
2 | HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1309+192A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 8/10 | chr5 | 65596859 | |||||||
| chr5:65596935 | T | A | 1 | a0001c0001t0001g0023 | 2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1309+116A>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 8/10 | chr5 | 65596935 | |||||||
| chr5:65597201 | A | G | 1 | a0001c0008t0030g0073 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1180-21T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65597201 | |||||||
| chr5:65597372 | GACC | G | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1180-195_1180-193d others(5): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65597372 | |||||||
| chr5:65597482 | A | C | 1 | a0001c0001t0033g0195 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1180-302T>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65597482 | |||||||
| chr5:65597615 | A | C | 1 | a0001c0001t0041g0140 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1180-435T>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65597615 | |||||||
| chr5:65597616 | A | AT | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(30): Show |
68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1180-437dupA | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65597616 | |||||||
| chr5:65597625 | T | A | 4 | a0001c0001t0010g0005 a0001c0001t0010g0148 a0001c0001t0019g0143 others(1): Show |
8 | HG02486.hp1 HG02647.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180-445A>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65597625 | |||||||
| chr5:65597626 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1180-446T>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65597626 | |||||||
| chr5:65597700 | T | C | 1 | a0001c0008t0030g0073 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1180-520A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65597700 | |||||||
| chr5:65597780 | G | A | 1 | a0001c0001t0007g0078 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1180-600C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65597780 | |||||||
| chr5:65597829 | T | G | 1 | a0001c0001t0001g0098 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1180-649A>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65597829 | |||||||
| chr5:65598072 | C | T | 33 | a0001c0001t0004g0006 a0001c0001t0004g0044 a0001c0001t0004g0045 others(30): Show |
47 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.1180-892G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65598072 | |||||||
| chr5:65598113 | T | C | 1 | a0001c0008t0030g0073 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1180-933A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65598113 | |||||||
| chr5:65598227 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0007g0078 |
2 | HG02257.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1180-1047G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65598227 | |||||||
| chr5:65598277 | A | G | 2 | a0001c0002t0011g0119 a0001c0002t0015g0118 |
2 | NA18959.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1180-1097T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65598277 | |||||||
| chr5:65598323 | G | A | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(30): Show |
68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1180-1143C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65598323 | |||||||
| chr5:65598455 | C | T | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1180-1275G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65598455 | |||||||
| chr5:65598473 | G | A | 26 | a0001c0002t0006g0008 a0001c0002t0006g0033 a0001c0002t0006g0121 others(23): Show |
31 | HG00741.hp2 HG01256.hp2 HG01952.hp1 others(28): Show |
intron_variant | MODIFIER | c.1180-1293C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65598473 | |||||||
| chr5:65598481 | T | C | 1 | a0001c0002t0011g0136 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1180-1301A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65598481 | |||||||
| chr5:65598547 | C | T | 1 | a0001c0001t0004g0174 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1180-1367G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65598547 | |||||||
| chr5:65598566 | A | G | 4 | a0001c0002t0021g0042 a0001c0002t0021g0170 a0001c0002t0027g0043 others(1): Show |
6 | HG01109.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1180-1386T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65598566 | |||||||
| chr5:65598578 | C | T | 24 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0034 others(21): Show |
43 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.1180-1398G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65598578 | |||||||
| chr5:65598617 | C | T | 66 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(63): Show |
115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1180-1437G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65598617 | |||||||
| chr5:65598621 | C | T | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1180-1441G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65598621 | |||||||
| chr5:65598667 | G | A | 1 | a0001c0001t0005g0155 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1180-1487C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65598667 | |||||||
| chr5:65598690 | G | A | 5 | a0001c0001t0005g0213 a0001c0001t0005g0214 a0001c0001t0005g0216 others(2): Show |
5 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-1510C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65598690 | |||||||
| chr5:65598735 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1180-1555G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65598735 | |||||||
| chr5:65598743 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1180-1563G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65598743 | |||||||
| chr5:65598744 | G | A | 1 | a0001c0001t0003g0160 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1180-1564C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65598744 | |||||||
| chr5:65598748 | CA | C | 160 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0023 others(157): Show |
245 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.1180-1569delT | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65598748 | |||||||
| chr5:65598884 | T | C | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(30): Show |
68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1180-1704A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65598884 | |||||||
| chr5:65599084 | G | A | 155 | a0001c0001t0001g0023 a0001c0001t0001g0076 a0001c0001t0002g0002 others(152): Show |
241 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1180-1904C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65599084 | |||||||
| chr5:65599127 | A | G | 1 | a0001c0001t0041g0140 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1180-1947T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65599127 | |||||||
| chr5:65599146 | AT | A | 2 | a0001c0001t0002g0054 a0001c0001t0002g0205 |
3 | HG01192.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1180-1967delA | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65599146 | |||||||
| chr5:65599150 | TCTTGTAT others(10): Show |
T | 2 | a0001c0001t0002g0054 a0001c0001t0002g0205 |
3 | HG01192.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1180-1987_1180-197 others(21): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65599150 | |||||||
| chr5:65599174 | A | C | 1 | a0002c0004t0001g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1180-1994T>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65599174 | |||||||
| chr5:65599418 | C | G | 1 | a0001c0001t0002g0053 | 2 | NA18970.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1180-2238G>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65599418 | |||||||
| chr5:65599466 | C | T | 2 | a0001c0001t0004g0183 a0001c0001t0004g0190 |
2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1180-2286G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65599466 | |||||||
| chr5:65599481 | C | CTTTTAAT others(19): Show |
1 | a0001c0001t0001g0090 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1180-2327_1180-230 others(30): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65599481 | |||||||
| chr5:65599613 | T | C | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(30): Show |
68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1180-2433A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65599613 | |||||||
| chr5:65599672 | T | C | 4 | a0001c0001t0005g0039 a0001c0001t0005g0145 a0001c0001t0005g0156 others(1): Show |
5 | HG02055.hp2 HG02258.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-2492A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65599672 | |||||||
| chr5:65599734 | A | G | 2 | a0001c0001t0018g0041 a0001c0001t0018g0167 |
3 | HG02258.hp2 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1180-2554T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65599734 | |||||||
| chr5:65599792 | G | A | 2 | a0001c0006t0001g0074 a0001c0006t0001g0075 |
2 | HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1180-2612C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65599792 | |||||||
| chr5:65599916 | G | C | 5 | a0001c0001t0010g0005 a0001c0001t0010g0148 a0001c0001t0019g0143 others(2): Show |
9 | HG02486.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1180-2736C>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65599916 | |||||||
| chr5:65600307 | A | C | 1 | a0001c0001t0018g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1180-3127T>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65600307 | |||||||
| chr5:65600488 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1180-3308G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65600488 | |||||||
| chr5:65600622 | T | TA | 49 | a0001c0001t0001g0013 a0001c0001t0001g0063 a0001c0001t0001g0079 others(46): Show |
76 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.1180-3443dupT | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65600622 | |||||||
| chr5:65600622 | T | TAAA | 29 | a0001c0001t0004g0006 a0001c0001t0004g0044 a0001c0001t0004g0051 others(26): Show |
41 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.1180-3445_1180-344 others(7): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65600622 | |||||||
| chr5:65600721 | T | C | 1 | a0001c0001t0001g0023 | 2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1180-3541A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65600721 | |||||||
| chr5:65600862 | T | C | 1 | a0001c0002t0040g0131 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1180-3682A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65600862 | |||||||
| chr5:65600959 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1180-3779G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65600959 | |||||||
| chr5:65600976 | A | C | 35 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0034 others(32): Show |
56 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1180-3796T>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65600976 | |||||||
| chr5:65601228 | G | A | 148 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(145): Show |
233 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.1179+3683C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65601228 | |||||||
| chr5:65601488 | A | G | 4 | a0001c0001t0005g0039 a0001c0001t0005g0145 a0001c0001t0005g0156 others(1): Show |
5 | HG02055.hp2 HG02258.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179+3423T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65601488 | |||||||
| chr5:65601509 | A | G | 7 | a0001c0001t0003g0158 a0001c0001t0003g0160 a0001c0001t0005g0159 others(4): Show |
8 | HG01261.hp2 HG02132.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1179+3402T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65601509 | |||||||
| chr5:65601721 | CA | C | 33 | a0001c0001t0004g0006 a0001c0001t0004g0044 a0001c0001t0004g0045 others(30): Show |
47 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.1179+3189delT | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65601721 | |||||||
| chr5:65601767 | T | C | 1 | a0001c0002t0011g0117 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1179+3144A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65601767 | |||||||
| chr5:65602096 | T | A | 1 | a0001c0001t0003g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1179+2815A>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65602096 | |||||||
| chr5:65602127 | A | T | 33 | a0001c0001t0004g0006 a0001c0001t0004g0044 a0001c0001t0004g0045 others(30): Show |
47 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.1179+2784T>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65602127 | |||||||
| chr5:65602236 | C | A | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1179+2675G>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65602236 | |||||||
| chr5:65602248 | C | T | 1 | a0001c0006t0001g0074 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1179+2663G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65602248 | |||||||
| chr5:65602347 | G | A | 30 | a0001c0002t0006g0008 a0001c0002t0006g0033 a0001c0002t0006g0121 others(27): Show |
37 | HG00741.hp2 HG01109.hp1 HG01256.hp2 others(34): Show |
intron_variant | MODIFIER | c.1179+2564C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65602347 | |||||||
| chr5:65602415 | C | T | 5 | a0001c0001t0005g0213 a0001c0001t0005g0214 a0001c0001t0005g0216 others(2): Show |
5 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179+2496G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65602415 | |||||||
| chr5:65602447 | G | A | 1 | a0001c0001t0003g0037 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1179+2464C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65602447 | |||||||
| chr5:65602551 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1179+2360G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65602551 | |||||||
| chr5:65602602 | T | A | 33 | a0001c0001t0004g0006 a0001c0001t0004g0044 a0001c0001t0004g0045 others(30): Show |
47 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.1179+2309A>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65602602 | |||||||
| chr5:65602642 | G | A | 3 | a0001c0001t0001g0099 a0001c0001t0005g0156 a0001c0001t0010g0139 |
3 | HG00408.hp1 HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1179+2269C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65602642 | |||||||
| chr5:65602767 | A | G | 5 | a0002c0004t0001g0060 a0002c0004t0001g0065 a0002c0004t0001g0068 others(2): Show |
5 | HG02630.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1179+2144T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65602767 | |||||||
| chr5:65603043 | T | G | 1 | a0001c0001t0001g0061 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1179+1868A>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65603043 | |||||||
| chr5:65603204 | T | C | 2 | a0001c0001t0007g0010 a0001c0001t0007g0069 |
4 | HG02970.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1179+1707A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65603204 | |||||||
| chr5:65603222 | CTGTT | C | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1179+1685_1179+168 others(8): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65603222 | |||||||
| chr5:65603314 | G | A | 1 | a0001c0002t0006g0132 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1179+1597C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65603314 | |||||||
| chr5:65603392 | C | T | 46 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0034 others(43): Show |
71 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.1179+1519G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65603392 | |||||||
| chr5:65603401 | G | A | 30 | a0001c0002t0006g0008 a0001c0002t0006g0033 a0001c0002t0006g0121 others(27): Show |
37 | HG00741.hp2 HG01109.hp1 HG01256.hp2 others(34): Show |
intron_variant | MODIFIER | c.1179+1510C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65603401 | |||||||
| chr5:65603565 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0007g0100 a0001c0006t0001g0074 others(1): Show |
5 | HG01243.hp2 HG02622.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1179+1346A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65603565 | |||||||
| chr5:65603622 | T | C | 1 | a0001c0001t0001g0023 | 2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1179+1289A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65603622 | |||||||
| chr5:65603703 | C | A | 2 | a0001c0001t0007g0010 a0001c0001t0007g0069 |
4 | HG02970.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1179+1208G>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65603703 | |||||||
| chr5:65603811 | C | T | 1 | a0001c0001t0003g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1179+1100G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65603811 | |||||||
| chr5:65603934 | CT | C | 5 | a0002c0004t0001g0060 a0002c0004t0001g0065 a0002c0004t0001g0068 others(2): Show |
5 | HG02630.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1179+976delA | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65603934 | |||||||
| chr5:65603962 | C | CT | 153 | a0001c0001t0001g0023 a0001c0001t0001g0076 a0001c0001t0001g0088 others(150): Show |
238 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.1179+948dupA | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65603962 | |||||||
| chr5:65604080 | C | T | 1 | a0001c0001t0001g0007 | 4 | HG00735.hp1 HG00741.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.1179+831G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65604080 | |||||||
| chr5:65604106 | T | C | 4 | a0001c0003t0013g0011 a0001c0003t0013g0070 a0001c0003t0013g0071 others(1): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1179+805A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65604106 | |||||||
| chr5:65604119 | AG | A | 6 | a0001c0001t0007g0010 a0001c0001t0007g0069 a0001c0003t0013g0011 others(3): Show |
10 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1179+791delC | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65604119 | |||||||
| chr5:65604145 | G | A | 1 | a0001c0002t0006g0133 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1179+766C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65604145 | |||||||
| chr5:65604158 | G | A | 4 | a0001c0003t0013g0011 a0001c0003t0013g0070 a0001c0003t0013g0071 others(1): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1179+753C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65604158 | |||||||
| chr5:65604391 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1179+520C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65604391 | |||||||
| chr5:65604415 | A | T | 26 | a0001c0002t0006g0008 a0001c0002t0006g0033 a0001c0002t0006g0121 others(23): Show |
31 | HG00741.hp2 HG01256.hp2 HG01952.hp1 others(28): Show |
intron_variant | MODIFIER | c.1179+496T>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65604415 | |||||||
| chr5:65604452 | A | T | 5 | a0001c0001t0005g0213 a0001c0001t0005g0214 a0001c0001t0005g0216 others(2): Show |
5 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179+459T>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65604452 | |||||||
| chr5:65604619 | T | C | 45 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0034 others(42): Show |
70 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.1179+292A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65604619 | |||||||
| chr5:65604623 | T | C | 2 | a0001c0006t0001g0074 a0001c0006t0001g0075 |
2 | HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1179+288A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 7/10 | chr5 | 65604623 | |||||||
| chr5:65605048 | A | G | 1 | a0001c0001t0041g0140 | 1 | HG02559.hp1 | splice_region_variant&intron_variant | LOW | c.1045-3T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65605048 | |||||||
| chr5:65605148 | A | C | 1 | a0001c0001t0041g0140 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1045-103T>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65605148 | |||||||
| chr5:65605175 | A | G | 149 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(146): Show |
234 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.1045-130T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65605175 | |||||||
| chr5:65605278 | A | C | 1 | a0001c0001t0002g0053 | 2 | NA18970.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1045-233T>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65605278 | |||||||
| chr5:65605591 | T | C | 111 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(108): Show |
172 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.1045-546A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65605591 | |||||||
| chr5:65605591 | T | G | 31 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0034 others(28): Show |
51 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1045-546A>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65605591 | |||||||
| chr5:65605719 | CAT | C | 4 | a0001c0003t0013g0011 a0001c0003t0013g0070 a0001c0003t0013g0071 others(1): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045-676_1045-675d others(4): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65605719 | |||||||
| chr5:65605747 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1045-702C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65605747 | |||||||
| chr5:65605826 | T | C | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1045-781A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65605826 | |||||||
| chr5:65605839 | C | T | 4 | a0001c0001t0005g0213 a0001c0001t0005g0214 a0001c0001t0005g0216 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1045-794G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65605839 | |||||||
| chr5:65605901 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1045-856G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65605901 | |||||||
| chr5:65606019 | G | A | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1045-974C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65606019 | |||||||
| chr5:65606264 | C | T | 112 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(109): Show |
186 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1045-1219G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65606264 | |||||||
| chr5:65606280 | C | T | 33 | a0001c0001t0004g0006 a0001c0001t0004g0044 a0001c0001t0004g0045 others(30): Show |
47 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.1045-1235G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65606280 | |||||||
| chr5:65606382 | G | A | 66 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(63): Show |
115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1045-1337C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65606382 | |||||||
| chr5:65606441 | C | T | 30 | a0001c0002t0006g0008 a0001c0002t0006g0033 a0001c0002t0006g0121 others(27): Show |
37 | HG00741.hp2 HG01109.hp1 HG01256.hp2 others(34): Show |
intron_variant | MODIFIER | c.1045-1396G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65606441 | |||||||
| chr5:65606451 | C | A | 3 | a0001c0001t0002g0021 a0001c0001t0002g0194 a0001c0001t0017g0197 |
5 | NA18992.hp1 NA18998.hp2 NA19070.hp1 others(2): Show |
intron_variant | MODIFIER | c.1045-1406G>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65606451 | |||||||
| chr5:65606465 | G | A | 33 | a0001c0001t0004g0006 a0001c0001t0004g0044 a0001c0001t0004g0045 others(30): Show |
47 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.1045-1420C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65606465 | |||||||
| chr5:65606468 | C | CA | 7 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0105 others(4): Show |
9 | HG00673.hp1 HG02148.hp2 HG03831.hp2 others(6): Show |
intron_variant | MODIFIER | c.1045-1424dupT | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65606468 | |||||||
| chr5:65606483 | AAC | A | 13 | a0001c0001t0002g0205 a0001c0001t0004g0051 a0001c0001t0004g0183 others(10): Show |
14 | HG01515.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1045-1440_1045-143 others(6): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65606483 | |||||||
| chr5:65606484 | AC | A | 94 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(91): Show |
149 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1045-1440delG | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65606484 | |||||||
| chr5:65606485 | C | A | 39 | a0001c0001t0002g0057 a0001c0001t0002g0199 a0001c0001t0003g0003 others(36): Show |
60 | HG00438.hp1 HG00558.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1045-1440G>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65606485 | |||||||
| chr5:65606699 | C | T | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(30): Show |
68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1045-1654G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65606699 | |||||||
| chr5:65606958 | ACT | A | 2 | a0001c0001t0007g0010 a0001c0001t0007g0069 |
4 | HG02970.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1045-1915_1045-191 others(6): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65606958 | |||||||
| chr5:65606981 | C | A | 1 | a0001c0001t0003g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1045-1936G>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65606981 | |||||||
| chr5:65606984 | A | T | 2 | a0001c0001t0007g0010 a0001c0001t0007g0069 |
4 | HG02970.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1045-1939T>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65606984 | |||||||
| chr5:65607477 | C | G | 1 | a0001c0001t0001g0023 | 2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1044+1766G>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65607477 | |||||||
| chr5:65607565 | C | T | 2 | a0001c0001t0018g0041 a0001c0001t0018g0167 |
3 | HG02258.hp2 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1044+1678G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65607565 | |||||||
| chr5:65607589 | C | T | 33 | a0001c0001t0004g0006 a0001c0001t0004g0044 a0001c0001t0004g0045 others(30): Show |
47 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.1044+1654G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65607589 | |||||||
| chr5:65607759 | T | A | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1044+1484A>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65607759 | |||||||
| chr5:65607846 | A | C | 1 | a0001c0001t0007g0078 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1044+1397T>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65607846 | |||||||
| chr5:65607945 | G | C | 1 | a0001c0001t0041g0140 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1044+1298C>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65607945 | |||||||
| chr5:65608161 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1044+1082G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65608161 | |||||||
| chr5:65608323 | A | T | 45 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0034 others(42): Show |
70 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.1044+920T>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65608323 | |||||||
| chr5:65608430 | G | A | 4 | a0001c0001t0003g0158 a0001c0001t0003g0160 a0001c0001t0005g0159 others(1): Show |
4 | HG02132.hp1 NA18973.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044+813C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65608430 | |||||||
| chr5:65608436 | G | A | 1 | a0001c0001t0001g0027 | 2 | NA18974.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1044+807C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65608436 | |||||||
| chr5:65608442 | G | T | 1 | a0001c0001t0001g0023 | 2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1044+801C>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65608442 | |||||||
| chr5:65608469 | C | A | 4 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG01243.hp1 HG02818.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044+774G>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65608469 | |||||||
| chr5:65608502 | C | A | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1044+741G>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65608502 | |||||||
| chr5:65608802 | C | G | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1044+441G>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65608802 | |||||||
| chr5:65608944 | G | GA | 35 | a0001c0001t0001g0082 a0001c0001t0001g0102 a0001c0001t0002g0206 others(32): Show |
49 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1044+298dupT | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65608944 | |||||||
| chr5:65609013 | G | A | 1 | a0001c0001t0003g0141 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1044+230C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 6/10 | chr5 | 65609013 | |||||||
| chr5:65609673 | T | A | 4 | a0001c0003t0013g0011 a0001c0003t0013g0070 a0001c0003t0013g0071 others(1): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.829-215A>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 5/10 | chr5 | 65609673 | |||||||
| chr5:65609713 | G | A | 30 | a0001c0002t0006g0008 a0001c0002t0006g0033 a0001c0002t0006g0121 others(27): Show |
37 | HG00741.hp2 HG01109.hp1 HG01256.hp2 others(34): Show |
intron_variant | MODIFIER | c.829-255C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 5/10 | chr5 | 65609713 | |||||||
| chr5:65609717 | G | A | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(30): Show |
68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.829-259C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 5/10 | chr5 | 65609717 | |||||||
| chr5:65609894 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.829-436T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 5/10 | chr5 | 65609894 | |||||||
| chr5:65609953 | G | C | 149 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(146): Show |
234 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.829-495C>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 5/10 | chr5 | 65609953 | |||||||
| chr5:65610220 | A | C | 1 | a0001c0003t0013g0070 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.828+641T>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 5/10 | chr5 | 65610220 | |||||||
| chr5:65610231 | T | C | 33 | a0001c0001t0004g0006 a0001c0001t0004g0044 a0001c0001t0004g0045 others(30): Show |
47 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.828+630A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 5/10 | chr5 | 65610231 | |||||||
| chr5:65610284 | T | C | 45 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0034 others(42): Show |
70 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.828+577A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 5/10 | chr5 | 65610284 | |||||||
| chr5:65610397 | T | C | 1 | a0001c0001t0007g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.828+464A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 5/10 | chr5 | 65610397 | |||||||
| chr5:65610534 | G | C | 1 | a0001c0001t0001g0007 | 4 | HG00735.hp1 HG00741.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.828+327C>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 5/10 | chr5 | 65610534 | |||||||
| chr5:65610561 | C | T | 1 | a0001c0001t0009g0198 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.828+300G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 5/10 | chr5 | 65610561 | |||||||
| chr5:65610790 | T | A | 162 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0023 others(159): Show |
251 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.828+71A>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 5/10 | chr5 | 65610790 | |||||||
| chr5:65610794 | T | A | 1 | a0001c0001t0001g0103 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.828+67A>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 5/10 | chr5 | 65610794 | |||||||
| chr5:65611058 | A | G | 1 | a0001c0001t0022g0149 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.646-15T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 4/10 | chr5 | 65611058 | |||||||
| chr5:65611138 | G | A | 1 | a0001c0001t0014g0189 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.646-95C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 4/10 | chr5 | 65611138 | |||||||
| chr5:65611237 | G | A | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.646-194C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 4/10 | chr5 | 65611237 | |||||||
| chr5:65611415 | GT | G | 5 | a0001c0001t0001g0023 a0001c0001t0001g0081 a0001c0001t0004g0190 others(2): Show |
6 | HG01243.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.645+187delA | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 4/10 | chr5 | 65611415 | |||||||
| chr5:65611450 | T | C | 1 | a0001c0002t0006g0134 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.645+153A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 4/10 | chr5 | 65611450 | |||||||
| chr5:65611480 | T | C | 2 | a0001c0001t0007g0010 a0001c0001t0007g0069 |
4 | HG02970.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+123A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 4/10 | chr5 | 65611480 | |||||||
| chr5:65611903 | C | T | 1 | a0001c0001t0041g0140 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.367-22G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 3/10 | chr5 | 65611903 | |||||||
| chr5:65612058 | G | C | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.367-177C>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 3/10 | chr5 | 65612058 | |||||||
| chr5:65612129 | T | C | 5 | a0001c0001t0010g0005 a0001c0001t0010g0148 a0001c0001t0019g0143 others(2): Show |
9 | HG02486.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.367-248A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 3/10 | chr5 | 65612129 | |||||||
| chr5:65612146 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0067 |
4 | HG02451.hp2 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.367-265G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 3/10 | chr5 | 65612146 | |||||||
| chr5:65612284 | T | G | 112 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(109): Show |
186 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.367-403A>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 3/10 | chr5 | 65612284 | |||||||
| chr5:65612449 | C | G | 1 | a0001c0001t0001g0027 | 2 | NA18974.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.367-568G>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 3/10 | chr5 | 65612449 | |||||||
| chr5:65612523 | T | TA | 35 | a0001c0001t0005g0213 a0001c0001t0005g0214 a0001c0001t0005g0216 others(32): Show |
42 | HG00741.hp2 HG01109.hp1 HG01256.hp2 others(39): Show |
intron_variant | MODIFIER | c.367-643dupT | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 3/10 | chr5 | 65612523 | |||||||
| chr5:65612660 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0007g0078 |
2 | HG02257.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.367-779G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 3/10 | chr5 | 65612660 | |||||||
| chr5:65612775 | C | T | 3 | a0001c0002t0021g0042 a0001c0002t0021g0170 a0001c0002t0049g0169 |
4 | HG01109.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-894G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 3/10 | chr5 | 65612775 | |||||||
| chr5:65612811 | T | A | 1 | a0001c0001t0005g0217 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.367-930A>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 3/10 | chr5 | 65612811 | |||||||
| chr5:65612907 | T | C | 1 | a0001c0001t0018g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.367-1026A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 3/10 | chr5 | 65612907 | |||||||
| chr5:65613164 | G | T | 1 | a0001c0001t0001g0023 | 2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.366+934C>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 3/10 | chr5 | 65613164 | |||||||
| chr5:65613216 | AC | A | 5 | a0001c0001t0010g0005 a0001c0001t0010g0148 a0001c0001t0019g0143 others(2): Show |
9 | HG02486.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.366+881delG | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 3/10 | chr5 | 65613216 | |||||||
| chr5:65613239 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.366+859A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 3/10 | chr5 | 65613239 | |||||||
| chr5:65613289 | A | T | 1 | a0001c0001t0007g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.366+809T>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 3/10 | chr5 | 65613289 | |||||||
| chr5:65613308 | T | G | 27 | a0001c0002t0006g0008 a0001c0002t0006g0033 a0001c0002t0006g0121 others(24): Show |
33 | HG00741.hp2 HG01256.hp2 HG01952.hp1 others(30): Show |
intron_variant | MODIFIER | c.366+790A>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 3/10 | chr5 | 65613308 | |||||||
| chr5:65613309 | G | A | 1 | a0001c0001t0012g0191 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.366+789C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 3/10 | chr5 | 65613309 | |||||||
| chr5:65613440 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.366+658G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 3/10 | chr5 | 65613440 | |||||||
| chr5:65613660 | A | G | 66 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(63): Show |
115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.366+438T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 3/10 | chr5 | 65613660 | |||||||
| chr5:65614565 | T | C | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(30): Show |
68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.245-346A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65614565 | |||||||
| chr5:65614578 | T | C | 112 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(109): Show |
186 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.245-359A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65614578 | |||||||
| chr5:65614659 | C | T | 4 | a0001c0003t0013g0011 a0001c0003t0013g0070 a0001c0003t0013g0071 others(1): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-440G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65614659 | |||||||
| chr5:65614734 | C | CA | 6 | a0001c0001t0001g0063 a0001c0001t0001g0105 a0001c0001t0001g0112 others(3): Show |
9 | HG00741.hp2 HG01243.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.245-516dupT | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65614734 | |||||||
| chr5:65614903 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.245-684A>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65614903 | |||||||
| chr5:65614941 | A | G | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.245-722T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65614941 | |||||||
| chr5:65614955 | T | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0079 |
3 | HG01243.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.245-736A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65614955 | |||||||
| chr5:65615017 | C | A | 66 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(63): Show |
115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.245-798G>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65615017 | |||||||
| chr5:65615087 | G | C | 1 | a0001c0001t0003g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.245-868C>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65615087 | |||||||
| chr5:65615134 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.245-915A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65615134 | |||||||
| chr5:65615289 | G | T | 2 | a0001c0001t0007g0010 a0001c0001t0007g0069 |
4 | HG02970.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-1070C>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65615289 | |||||||
| chr5:65615527 | T | TA | 145 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(142): Show |
228 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.245-1309dupT | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65615527 | |||||||
| chr5:65615644 | A | G | 1 | a0001c0001t0001g0026 | 2 | HG01975.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.245-1425T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65615644 | |||||||
| chr5:65615650 | T | C | 66 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(63): Show |
115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.245-1431A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65615650 | |||||||
| chr5:65615707 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.245-1488T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65615707 | |||||||
| chr5:65615788 | T | G | 1 | a0001c0001t0002g0194 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.245-1569A>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65615788 | |||||||
| chr5:65615927 | C | G | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(30): Show |
68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.245-1708G>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65615927 | |||||||
| chr5:65615985 | AAGG | A | 3 | a0001c0001t0003g0161 a0001c0001t0003g0163 a0001c0001t0031g0162 |
3 | HG01167.hp2 HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.245-1769_245-1767d others(5): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65615985 | |||||||
| chr5:65616069 | T | A | 1 | a0001c0002t0006g0033 | 2 | HG02698.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.245-1850A>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65616069 | |||||||
| chr5:65616099 | C | T | 1 | a0001c0001t0017g0197 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.245-1880G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65616099 | |||||||
| chr5:65616100 | G | A | 2 | a0001c0002t0006g0008 a0001c0002t0011g0136 |
5 | HG00741.hp2 HG02145.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-1881C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65616100 | |||||||
| chr5:65616150 | G | C | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(30): Show |
68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.245-1931C>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65616150 | |||||||
| chr5:65616256 | C | T | 5 | a0001c0001t0010g0005 a0001c0001t0010g0148 a0001c0001t0019g0143 others(2): Show |
9 | HG02486.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.244+1837G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65616256 | |||||||
| chr5:65616623 | C | T | 4 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG01243.hp1 HG02818.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+1470G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65616623 | |||||||
| chr5:65616641 | T | TA | 6 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0067 others(3): Show |
10 | HG02027.hp1 HG02451.hp2 HG03516.hp2 others(7): Show |
intron_variant | MODIFIER | c.244+1451dupT | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65616641 | |||||||
| chr5:65616641 | TA | T | 75 | a0001c0001t0001g0025 a0001c0001t0001g0076 a0001c0001t0001g0111 others(72): Show |
108 | HG00438.hp1 HG00642.hp1 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.244+1451delT | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65616641 | |||||||
| chr5:65616641 | TAA | T | 35 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(32): Show |
69 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.244+1450_244+1451d others(4): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65616641 | |||||||
| chr5:65616641 | TAAAAAAA others(4): Show |
T | 2 | a0001c0001t0003g0034 a0001c0001t0003g0142 |
3 | HG00733.hp2 HG00735.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.244+1441_244+1451d others(13): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65616641 | |||||||
| chr5:65616663 | A | G | 1 | a0001c0001t0007g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.244+1430T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65616663 | |||||||
| chr5:65616713 | A | G | 1 | a0001c0001t0041g0140 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.244+1380T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65616713 | |||||||
| chr5:65617050 | T | C | 148 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(145): Show |
233 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.244+1043A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65617050 | |||||||
| chr5:65617070 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.244+1023A>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65617070 | |||||||
| chr5:65617117 | T | TTTCTTGG others(24): Show |
2 | a0001c0001t0020g0209 a0001c0001t0037g0208 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.244+945_244+975dup others(31): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65617117 | |||||||
| chr5:65617122 | T | C | 1 | a0001c0002t0011g0137 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.244+971A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65617122 | |||||||
| chr5:65617173 | G | C | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(30): Show |
68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.244+920C>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65617173 | |||||||
| chr5:65617205 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0109 |
4 | HG00609.hp1 HG02027.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+888C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65617205 | |||||||
| chr5:65617510 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.244+583G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65617510 | |||||||
| chr5:65617517 | T | C | 33 | a0001c0001t0004g0006 a0001c0001t0004g0044 a0001c0001t0004g0045 others(30): Show |
47 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.244+576A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65617517 | |||||||
| chr5:65617523 | A | C | 2 | a0001c0006t0001g0074 a0001c0006t0001g0075 |
2 | HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.244+570T>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65617523 | |||||||
| chr5:65617601 | C | T | 1 | a0001c0008t0030g0073 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.244+492G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65617601 | |||||||
| chr5:65617662 | A | C | 23 | a0001c0002t0006g0033 a0001c0002t0006g0121 a0001c0002t0006g0129 others(20): Show |
25 | HG01256.hp2 HG01952.hp1 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.244+431T>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65617662 | |||||||
| chr5:65617775 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.244+318C>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65617775 | |||||||
| chr5:65617837 | G | A | 2 | a0001c0001t0007g0010 a0001c0001t0007g0069 |
4 | HG02970.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+256C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65617837 | |||||||
| chr5:65617929 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.244+164T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65617929 | |||||||
| chr5:65618014 | T | C | 30 | a0001c0002t0006g0008 a0001c0002t0006g0033 a0001c0002t0006g0121 others(27): Show |
37 | HG00741.hp2 HG01109.hp1 HG01256.hp2 others(34): Show |
intron_variant | MODIFIER | c.244+79A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 2/10 | chr5 | 65618014 | |||||||
| chr5:65618448 | A | T | 2 | a0001c0001t0007g0010 a0001c0001t0007g0069 |
4 | HG02970.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-193T>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65618448 | |||||||
| chr5:65618632 | T | C | 1 | a0001c0002t0027g0043 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.82-377A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65618632 | |||||||
| chr5:65618741 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.82-486T>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65618741 | |||||||
| chr5:65618767 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.82-512G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65618767 | |||||||
| chr5:65618817 | T | C | 2 | a0001c0001t0003g0166 a0001c0001t0023g0040 |
3 | NA18983.hp2 NA18991.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.82-562A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65618817 | |||||||
| chr5:65618934 | C | A | 1 | a0001c0001t0007g0078 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.82-679G>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65618934 | |||||||
| chr5:65619486 | G | A | 1 | a0001c0002t0015g0138 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.82-1231C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65619486 | |||||||
| chr5:65619575 | T | C | 2 | a0001c0001t0003g0016 a0001c0001t0003g0165 |
4 | HG01516.hp2 HG01517.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-1320A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65619575 | |||||||
| chr5:65619633 | C | T | 1 | a0001c0001t0002g0196 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.82-1378G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65619633 | |||||||
| chr5:65619796 | T | C | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(30): Show |
68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.82-1541A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65619796 | |||||||
| chr5:65619957 | G | A | 12 | a0001c0001t0004g0051 a0001c0001t0004g0183 a0001c0001t0004g0190 others(9): Show |
13 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.82-1702C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65619957 | |||||||
| chr5:65620048 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.82-1793C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65620048 | |||||||
| chr5:65620070 | A | G | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.82-1815T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65620070 | |||||||
| chr5:65620179 | G | A | 6 | a0001c0001t0002g0018 a0001c0001t0002g0059 a0001c0001t0002g0211 others(3): Show |
10 | HG00323.hp1 HG01255.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-1924C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65620179 | |||||||
| chr5:65620205 | A | T | 1 | a0001c0001t0002g0018 | 3 | HG00323.hp1 HG02257.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.82-1950T>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65620205 | |||||||
| chr5:65620263 | A | T | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.82-2008T>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65620263 | |||||||
| chr5:65620334 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0081 |
3 | NA18992.hp2 NA19063.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.82-2079G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65620334 | |||||||
| chr5:65620451 | T | C | 1 | a0001c0001t0041g0140 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.82-2196A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65620451 | |||||||
| chr5:65620521 | T | C | 33 | a0001c0001t0004g0006 a0001c0001t0004g0044 a0001c0001t0004g0045 others(30): Show |
47 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.82-2266A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65620521 | |||||||
| chr5:65620583 | A | AT | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.82-2329dupA | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65620583 | |||||||
| chr5:65620607 | C | A | 1 | a0002c0004t0001g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.82-2352G>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65620607 | |||||||
| chr5:65620647 | AT | A | 4 | a0001c0002t0021g0042 a0001c0002t0021g0170 a0001c0002t0027g0043 others(1): Show |
6 | HG01109.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-2393delA | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65620647 | |||||||
| chr5:65620648 | T | C | 33 | a0001c0001t0004g0006 a0001c0001t0004g0044 a0001c0001t0004g0045 others(30): Show |
47 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.82-2393A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65620648 | |||||||
| chr5:65620670 | A | G | 2 | a0001c0001t0002g0052 a0001c0001t0033g0195 |
3 | HG02683.hp2 HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.82-2415T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65620670 | |||||||
| chr5:65620742 | T | A | 2 | a0001c0001t0003g0166 a0001c0001t0023g0040 |
3 | NA18983.hp2 NA18991.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.82-2487A>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65620742 | |||||||
| chr5:65620789 | C | CA | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.82-2535_82-2534ins others(1): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65620789 | |||||||
| chr5:65620814 | A | G | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.82-2559T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65620814 | |||||||
| chr5:65620864 | C | T | 3 | a0001c0001t0005g0213 a0001c0001t0005g0214 a0001c0001t0019g0215 |
3 | HG01884.hp2 HG02145.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.82-2609G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65620864 | |||||||
| chr5:65620896 | C | A | 66 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(63): Show |
115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.82-2641G>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65620896 | |||||||
| chr5:65620912 | C | CA | 141 | a0001c0001t0001g0112 a0001c0001t0002g0002 a0001c0001t0002g0004 others(138): Show |
222 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.82-2658dupT | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65620912 | |||||||
| chr5:65621022 | C | A | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.82-2767G>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65621022 | |||||||
| chr5:65621054 | T | C | 1 | a0001c0001t0007g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.82-2799A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65621054 | |||||||
| chr5:65621167 | G | A | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.82-2912C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65621167 | |||||||
| chr5:65621213 | G | A | 2 | a0001c0001t0018g0041 a0001c0001t0018g0167 |
3 | HG02258.hp2 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.82-2958C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65621213 | |||||||
| chr5:65621335 | G | A | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.81+2859C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65621335 | |||||||
| chr5:65621385 | T | C | 1 | a0001c0001t0001g0022 | 2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.81+2809A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65621385 | |||||||
| chr5:65621405 | G | A | 45 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0034 others(42): Show |
70 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.81+2789C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65621405 | |||||||
| chr5:65621414 | T | C | 1 | a0001c0001t0022g0168 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.81+2780A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65621414 | |||||||
| chr5:65621426 | G | T | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.81+2768C>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65621426 | |||||||
| chr5:65621651 | C | A | 45 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0034 others(42): Show |
70 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.81+2543G>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65621651 | |||||||
| chr5:65621798 | G | GATT | 148 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(145): Show |
233 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.81+2395_81+2396ins others(3): Show |
TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65621798 | |||||||
| chr5:65621813 | G | A | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.81+2381C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65621813 | |||||||
| chr5:65621832 | A | T | 4 | a0001c0002t0021g0042 a0001c0002t0021g0170 a0001c0002t0027g0043 others(1): Show |
6 | HG01109.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+2362T>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65621832 | |||||||
| chr5:65621835 | A | T | 31 | a0001c0001t0001g0001 a0001c0001t0022g0168 a0001c0002t0006g0008 others(28): Show |
39 | HG00642.hp2 HG00741.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.81+2359T>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65621835 | |||||||
| chr5:65621838 | T | A | 66 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(63): Show |
115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.81+2356A>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65621838 | |||||||
| chr5:65621858 | C | G | 4 | a0001c0003t0013g0011 a0001c0003t0013g0070 a0001c0003t0013g0071 others(1): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+2336G>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65621858 | |||||||
| chr5:65621859 | A | T | 4 | a0001c0003t0013g0011 a0001c0003t0013g0070 a0001c0003t0013g0071 others(1): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+2335T>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65621859 | |||||||
| chr5:65622087 | C | T | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(30): Show |
68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.81+2107G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65622087 | |||||||
| chr5:65622137 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.81+2057A>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65622137 | |||||||
| chr5:65622188 | T | C | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(30): Show |
68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.81+2006A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65622188 | |||||||
| chr5:65622198 | C | T | 4 | a0001c0003t0013g0011 a0001c0003t0013g0070 a0001c0003t0013g0071 others(1): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+1996G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65622198 | |||||||
| chr5:65622600 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.81+1594G>A | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65622600 | |||||||
| chr5:65622686 | G | C | 5 | a0001c0001t0005g0213 a0001c0001t0005g0214 a0001c0001t0005g0216 others(2): Show |
5 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+1508C>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65622686 | |||||||
| chr5:65622717 | A | G | 1 | a0002c0004t0001g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.81+1477T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65622717 | |||||||
| chr5:65622721 | C | A | 1 | a0001c0001t0001g0079 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.81+1473G>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65622721 | |||||||
| chr5:65622794 | T | C | 1 | a0001c0001t0007g0078 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.81+1400A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65622794 | |||||||
| chr5:65623152 | A | G | 2 | a0001c0001t0007g0010 a0001c0001t0007g0069 |
4 | HG02970.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+1042T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65623152 | |||||||
| chr5:65623198 | A | G | 1 | a0001c0001t0010g0139 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.81+996T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65623198 | |||||||
| chr5:65623255 | A | G | 46 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0034 others(43): Show |
71 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.81+939T>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65623255 | |||||||
| chr5:65623553 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.81+641C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65623553 | |||||||
| chr5:65623623 | T | C | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.81+571A>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65623623 | |||||||
| chr5:65623631 | T | G | 5 | a0001c0001t0005g0213 a0001c0001t0005g0214 a0001c0001t0005g0216 others(2): Show |
5 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+563A>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65623631 | |||||||
| chr5:65623707 | TAC | T | 26 | a0001c0002t0006g0008 a0001c0002t0006g0033 a0001c0002t0006g0121 others(23): Show |
31 | HG00741.hp2 HG01256.hp2 HG01952.hp1 others(28): Show |
intron_variant | MODIFIER | c.81+485_81+486delGT | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65623707 | |||||||
| chr5:65623791 | C | A | 155 | a0001c0001t0001g0023 a0001c0001t0001g0076 a0001c0001t0002g0002 others(152): Show |
241 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.81+403G>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65623791 | |||||||
| chr5:65623941 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.81+253C>G | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65623941 | |||||||
| chr5:65624050 | C | G | 167 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0023 others(164): Show |
256 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.81+144G>C | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65624050 | |||||||
| chr5:65624164 | G | A | 142 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0018 others(139): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.81+30C>T | TRIM23 | ENSG00000113595.15 | transcript | ENST00000231524.14 | protein_coding | 1/10 | chr5 | 65624164 |